This Center brings together a number of investigators with specialties in pharmacokinetics, clinical pharmacology, analytical methodology, drug metabolism, medicine, laboratory medicine, pediatrics, dermatology and biostatistics. The overall area of concern of the group is to investigate and model the relationship between drug kinetics and dynamics and to discover, understand and quantify the modifications to drug kinetics and/or dynamics caused by altered physiology or pathology (disease states). Nine scientific units (and a core) examine and attempt to correlate input processes of drug into the body, distribution of drug into the general circulation and to sites of action, and drug loss processes with pharmacodynamic measures of pharmacologic effect, clinical effect and toxicity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM026691-08
Application #
3106050
Study Section
Pharmacology-Toxicology Review Committee (PTR)
Project Start
1979-08-01
Project End
1987-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
8
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Pharmacy
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Chen, Zhe; Brown, Emery N; Barbieri, Riccardo (2010) Characterizing nonlinear heartbeat dynamics within a point process framework. IEEE Trans Biomed Eng 57:1335-47
Chen, Zhe; Brown, Emery N; Barbieri, Riccardo (2009) Assessment of autonomic control and respiratory sinus arrhythmia using point process models of human heart beat dynamics. IEEE Trans Biomed Eng 56:1791-802
Egge-Jacobsen, Wolfgang; Unger, Matthias; Niemann, Claus U et al. (2004) Automated, fast, and sensitive quantification of drugs in human plasma by LC/LC-MS: quantification of 6 protease inhibitors and 3 nonnucleoside transcriptase inhibitors. Ther Drug Monit 26:546-62
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Serkova, N; Litt, L; Leibfritz, D et al. (2000) The novel immunosuppressant SDZ-RAD protects rat brain slices from cyclosporine-induced reduction of high-energy phosphates. Br J Pharmacol 129:485-92
Stanley, G B; Poolla, K; Siegel, R A (2000) Threshold modeling of autonomic control of heart rate variability. IEEE Trans Biomed Eng 47:1147-53
Christians, U; Jacobsen, W; Serkova, N et al. (2000) Automated, fast and sensitive quantification of drugs in blood by liquid chromatography-mass spectrometry with on-line extraction: immunosuppressants. J Chromatogr B Biomed Sci Appl 748:41-53
Jager, W; Correia, M A; Bornheim, L M et al. (1999) Ethynylestradiol-mediated induction of hepatic CYP3A9 in female rats: implication for cyclosporine metabolism. Drug Metab Dispos 27:1505-11

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